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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657146Generated: November 1, 2026

Water → 4-[(5,6,7,8-Tetrahydro-5,5,8,8-tetramethylnaphth-2-yl)ethynyl]-benzylamine

https://huagongshe.com/reaction/1657146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium SulfateHCID 24436—
Reactant4-[(5,6,7,8-Tetrahydro-5,5,8,8-tetramethylnaphth-2-yl)ethynyl]-benzonitrileHCID 13604826—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product4-[(5,6,7,8-Tetrahydro-5,5,8,8-tetramethylnaphth-2-yl)ethynyl]-benzylamineHCID 19786995—

Reaction Steps

A solution of 8.2 g (26 millimoles) of 4-[(5,6,7,8-tetrahydro-5,5,8,8-tetramethylnaphth-2-yl)-ethynyl]-benzonitrile (Example 1) in 150 ml of absolute ether was added dropwise to a suspension of 2.8 g (73 millimoles) of lithium aluminum hydride in 150 ml of absolute ether at room temperature in the course of 25 minutes. The mixture was stirred under reflux for 3.5 hours and then cooled, after which water was added carefully, sodium sulfate solution was added dropwise and the phases were separated. The aqueous phase was extracted twice with ether, and the combined ether phases were washed once with water, dried over Na2SO4 and evaporated down. 7.7 g (93%) of the title compound of melting point 84°-88° C. remained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256694
Source datasetuspto-grants-1993_10
ORD IDord-b2c6efcdc06242a08360ae63bb37cd52
Source noteuspto-grants-1993_10